Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
  • A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
  • A61K31/4164—1,3-Diazoles
  • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/12—Antihypertensives

Definitions

• the present invention is related to an orally disintegrating composition
• composition comprising compound of Formula I (Compound I) or pharmaceutically acceptable salts and/or esters thereof and one or more pharmaceutically acceptable excipient.
• the invention relates to methods for preparing the orally disintegrating compositions comprising Compound I and its use for preventing and/or treating hypertension in mammals, particularly in humans.
• Hypertension affects about 20% of the adult population in developed countries. In the adult population aged 60 years or older, this percentage increases to about 60% to 70% in general. Hypertension also is associated with an increased risk of other physiological complications including stroke, myocardial infarction, atrial fibrillation, heart failure, peripheral vascular disease and renal impairment. Although a number of antihypertensive drugs are available in various pharmacological categories, the efficacy and safety of such drugs can vary from patient to patient, in this regard new treatments are still a desired subject.
• Compound I which has a chemical name as 2-ethoxy-1-((2'-(5-oxo-2,5-dihydro-1,2,4-oxadiazol-3yl)-biphenyl-4-yl)methyl)-1 H-benzimidazole-7-carboxylic acid (hereinafter referred as "Compound I”) is an angiotensin II receptor antagonist and its chemical structure is shown in the Formula I.
• Angiotensin II receptor antagonists are used in the management of hypertension; they may have a particular role in patients who develop cough with ACE inhibitors. Some are also used in diabetic nephropathy and in the management of heart failure. They act mainly by selective blockade of AT1 receptors thus reducing the pressor effects of angiotension II.
• Known angiotension receptor II antagonists from the prior art are candesartan, eprosartan, irbesartan, losartan, olmesartan, telmisartan and valsartan.
• orally disintegrating formulations are becoming an increasingly important issue in the area of better patient compliance comparative to the conventional solid dosage forms for oral administration such as capsules and tablets.
• pediatric and geriatric patients frequently have difficulty in swallowing conventional solid dosage forms.
• the act of swallowing the medicament often requires fluids that increase gastric volume and the likelihood of nausea and vomiting. This occurs more often in hypertension patients.
• the orally disintegrating dosage form is one of the advantageous methods to deliver the drugs such as comprising angiotensin receptor II antagonists to such patients and provide a better patient compliance with recommended pharmaceutical therapies.
• the orally disintegrating dosage form is one of the advantageous methods to deliver the drugs to such patients.
• faster absorption of the drug occurs through buccal mucosa and it may reduce the first pass metabolism leading to better efficacy of the drug.
• This dosage form enhances the clinical effects of some drugs by leading to an increase in bioavailability and a reduction in side effects because of avoidance of first-pass liver metabolism.
• WO 99/25321 discloses immediate or modified release solid oral dosage forms where it is also aimed to provide high drug load tablets. This object is achieved by way of wet granulation resulting in anhydrous eprosartan which is stated to be useful in the preparation of high drug load tablets.
• potential disintegrants such as sodium starch glycolate, sodium carmellose and crosslinked polyvinyl pyrrolidone are cited, although a rapid release formulation is not exemplified. The examples further include crospovidone.
• potential diluents were also cited lactose, starch, mannitol, sorbitol, cellulose, inorganic sulfates and phosphates.
• orally disintegrating compositions would be desirable to improve patient compliance, particularly among elderly patients, because orally disintegrating compositions are easier to swallow and prevent "cheeking".
• a satisfied orally disintegrating dosage form needs to meet a number of requirements. Firstly, it has to disintegrate in the mouth spontaneously. The time in which a dosage form must dissolve or disintegrate in the oral cavity is necessarily much shorter than in the stomach. Moreover, a premature release in the mouth could also lead to problems due to the often unpleasant taste of the active ingredient. Besides, these compositions should be very porous and should not be very hard. These porous compositions tend to be very sensitive to humidity. As a consequence, they may have some stability problems.
• the formulation for a specific drug needs to be adapted in particular by a careful selection of the excipients used.
• the excipients selected may lead to formulations which are not bioavailable to the corresponding conventional dosage forms. Thus, they have to be chosen very carefully.
• compositions of Compound I or pharmaceutically acceptable salts and/or esters thereof which overcome above described problems and which further provide the advantageous property of allowing the active medicament to disintegrate or dissolve rapidly in the oral cavity which have a pleasant mouth feel and good mechanical strength, enough to be processed in high speed tableting machines and shipped in low cost packages.
• the main object of the present invention is to provide novel orally disintegrating composition
• a specific angiotensin II receptor antagonist such as Azilsartan which has a chemical name as 2-ethoxy-1-((2'-(5-oxo-2,5-dihydro-1,2,4-oxadiazol-3yl)-biphenyl-4-yl)methyl)-1H-benzimidazole-7-carboxylic acid (hereinafter reffered as "Compound I”) or pharmaceutically acceptable salts and/or esters thereof and one or more pharmaceutically acceptable excipient which overcomes the above described problems in prior art and have additive advantages over them.
• Compound I 2-ethoxy-1-((2'-(5-oxo-2,5-dihydro-1,2,4-oxadiazol-3yl)-biphenyl-4-yl)methyl)-1H-benzimidazole-7-carboxylic acid
• Compound I 2-ethoxy-1-((2'-(5-oxo-2
• Compound I is in the form of a medoxomil ester.
• Compound I is in the form of medoxomil ester and potassium salt.
• an orally disintegrating composition of Compound I is provided which is fundamentally comparable with the existing regular conventional solid dosage forms such as tablets or capsules, however with the unexpected benefits found with oral disintegration.
• the orally disintegrating composition of Compound I disintegrates in oral cavity in less than 90 seconds, preferably in less than 60 seconds, more preferably in less than 30 seconds.
• the orally disintegrating composition comprises Compound I or pharmaceutically acceptable salts and/or esters in an amount of 0.1 % to 80.0% by weight of total formulation, preferably in an amount of 1.0 % to 60.0%, the most preferably in an amount of 10.0% to 50.0%.
• Compound I is preferably in the form of medoxomil salt.
• compositions of this invention further comprising at least one pharmaceutically acceptable excipient selected from the group comprising super disintegrants, diluents, binders, lubricants, glidants, sweeteners, flavouring agents, preservatives and coloring agents.
• Suitable super disintegrants may include but not limited to crospovidone, croscarmellose sodium, low-substituted hydroxypropylcellulose, sodium starch glycollate and the like and mixtures thereof; preferably crospovidone.
• this orally disintegrating composition having a weight ratio of Compound I to super disintegrants, particularly crospovidone, in the range of between 1:10 and 10:1 (w/w), has a synergistic effect over the disintegration time.
• the range is between 1:5 and 5:1 (w/w).
• crospovidone has physical and chemical properties that make it ideal for constituting the appropriate disintegrant for this invention. Because crospovidone particles have a very different appearance from those of the other disintegrants. Crospovidone particles seem to consist of aggregates of smaller particles that are fused together. This aggregation gives crospovidone a spongy, highly porous appearance and it swells very little, yet takes water into its network quite rapidly. This helps crospovidone to dissolve easily and quickly in a little amount of water or saliva and makes its disintegrating rate much faster than other related excipients.
• crospovidone is present in an amount of between 0.10 to 30.0 % by weight, preferably in an amount of 3.0 to 15.0 % by weight of the total formulation and the formulation disintegrates in oral cavity in less than 90 seconds, preferably in less than 60 seconds, more preferably in less than 30 seconds.
• Suitable diluents may include but not limited to microcrystalline cellulose, mannitol, spray-dried mannitol, lactose, starch, sodium carbonate, sodium bicarbonate, calcium carbonate and the like and mixtures thereof; preferably spray-dried mannitol and/or microcrystalline cellulose.
• spray-dried mannitol has physical chemical properties that make it ideal for constituting the appropriate diluent for this invention. Because it dissolves easily and quickly in a little amount of water or saliva and its disintegrating rate is much faster than powder mannitol and other related saccharine excipients. It is highly compressible and it has optimum fluidity for direct compression processes. It has good dilution capacity due to the size and form of the particle, which makes it possible to accept large amounts of active ingredients that are not easily compressed. It is chemically very stable and non-hygroscopic.
• the amount of spray-dried mannitol is present from 1.0 to 60.% by weight of the orally disintegrating composition, preferably is present from 10.0 to 40.0% by weight of total composition.
• the amount of microcrystalline cellulose when the amount of microcrystalline cellulose is present from 1.0 to 30.0% by weight of the orally disintegrating composition, preferably it is present from 5.0 to 15.0% by weight, said amount makes it possible to significantly improve mechanical strength of the orally disintegrating tablet such as compressibility and hardness, also reduce friability. Higher quantities have negative impact on the palatability of the formula and lower quantities worsen the mechanical strength of the orally disintegrating tablet.
• the weight ratio of spray-dried mannitol to microcrystalline cellulose is in the range of between 1:10 and 10:1 (w/w), it has synergistic effect over the mechanical strength such as compressibility of Compound I and achieve a substantial reduction in disintegration time and have a good stability of the orally disintegrating composition.
• the range is between 1:5 and 5:1 (w/w).
• Suitable binders may include but not limited to polyvinylpyrrolidone, polyethylene glycol, polyvinyl alcohol, cellulose derivatives such as hydroxypropyl methyl cellulose, carboxy methyl cellulose, methyl cellulose, gelatin, polyvinylalcohol, carrageenan, guar gum, xanthan gum and the like and mixtures thereof; preferably the binder is polyvinylpyrrolidone and/or hydroxypropyl methyl cellulose. Binder content is from 1.0 to 20.0%, preferably from 2.0 to 10.0% by weight of total composition.
• Suitable lubricants may include but not limited to magnesium strearate, calcium stearate, sodium stearyl fumarate, sodium lauryl sulphate, stearic acid and the like and mixtures thereof; preferably the lubricant is magnesium strearate and sodium lauryl sulfate. Lubricant content is from 0.1 to 10.0% by weight of total composition.
• Suitable glidants may include but not limited to colloidal silicon dioxide, talc, aluminium silicate and the like and mixtures thereof; preferably the glidant is colloidal silicon dioxide. Glidant content is from 0.01 to 5.0% by weight of total composition.
• compositions of this invention may also include sweeteners and flavouring agents to improve patient compliance.
• Suitable sweeteners may include but not limited to aspartame, sucralose, saccharin, sugars such as glucose, lactose, fructose and sugar alcohols such as mannitol, sorbitol, xylitol, erythritol and the like and mixtures thereof; preferably the sweetner is aspartame, sucralose and/or saccharin.
• Sweetener content is from 0.01 to 5%, preferably from 0.10 to 3.0% by weight of total composition.
• Suitable flavoring agents may include but not limited to menthol, peppermint, cinnamon, chocolate, vanillin and fruit essences such as cherry, orange, strawberry, grape etc. and the like and mixtures thereof; preferably the flavouring agent is menthol and/or fruit essences.
• Flavouring agent content is from 0.01 to 5.0%, preferably from 0.10 to 3.0% by weight of total composition.
• menthol which due to its refreshing effect has a synergic effect with the spray-dried mannitol and a good tastemasking capacity due to its residual effect.
• Suitable preservatives may include but not limited to methyl paraben and propyl paraben and their salts (such as sodium, potassium), sodium benzoate, citric acid, benzoic acid, butylated hydroxytoluene and butylated hydroxyanisole and the like and mixtures thereof.
• Preservative content is from 0,01 to 5.0%, preferably from 0.1 to 2.0% by weight of total composition.
• Suiatable colouring agents may include but not limited to ferric oxide, FD&C (Food, Drug & Cosmetic) dyes, poncau and the like and mixtures thereof.
• a humidity absorbent agent may be added, such as precipitated silica in a proportion from 0.01 to 1.0% in weight of the total weight of the tablet, which may counteract the hydrophobicity of the active ingredient and improve the fluidity of the mixture.
• this present invention provides an orally disintegrating composition of compound I or pharmaceutically acceptable salts and/or esters thereof and one or more pharmaceutically acceptable excipients which is stable throughout the shelflife and which has high bioavailability.
• compositions of this invention include tablets, sachets, minitablets, multilayer and multicoated tablets, pellets or powders which can be formulated in accordance with methods that are standard in the art. It is preferably in the form of tablets.
• the present invention shows that it is possible to have a significant influence on the disintegration rate of the tablet by modifying the dimensions and shape of the tablet.
• the orally disintegrating composition will be weakened faster when it contacts with saliva, because the disintegration process is produced after wetting all the surface of the tablet via capillary action.
• any shape which maximizes the contact surface with the saliva may produce a significant reduction in disintegration time.
• the preferred shape of the orally disintegrating tablet composition of this invention may have a shape of a disk, circle, round, sphere, donut, bar, polygon, ellipse and the like.
• the preffered shape of the tablet is a flat round shape.
• the orally disintegrating compositions of the present invention may be prepared by conventional technology well known to those skilled in the art such as direct compression, dry granulation, wet granulation and the like.
• the orally disintegrating compositions of the present invention may also be prepared by other technologies such as spray drying, freeze drying, floss formation, molding, Zydis ® technology, Flashtab technology, OraSolv ® technology, DuraSolv ® technology, WowtabTM (With Out Water quick-dissolve tablet) technology and the like.
• Compound I or pharmaceutically acceptable salts and/or esters thereof, and other excipients are mixed together then the mixture is compressed to form tablets.
• the manufacturing process is preferably performed by mixing the components, blending the mixture with glidant(s) and lubricant(s) and compressing the blended mixture to form tablets.
• the process for preparing the orally disintegrating compositions of the invention comprises the following steps:
• Another embodiment of the present invention is to provide an orally disintegrating pharmaceutical dosage form comprising Compound I with one or more pharmaceutically acceptable excipient for preventing and/or treating hypertension in mammals, particularly in humans.
• Compound I can be administered in combination with diuretics, preferably the diuretics are selected from thiazide derivatives.
• said thiazide derivatives are selected from the group comprising hydrochlorothiazide, methylclothiazide, benzylhydrochlorothiazide, trichlormethiazide, cyclopenthiazide, polythiazide, ethiazide, cyclothiazide, bendroflumethiazide or hydroflumethiazide or mixtures thereof, preferably the thiazide is hydrochlorothiazide.
• the formulation for a specific drug needs to be adapted in particular by a careful selection of the excipients used.
• the excipients selected may lead to formulations which are not bioavailable to the corresponding conventional dosage forms. Thus, they have to be chosen very carefully.
• this orally disintegrating tablet composition has been designed, made up of the following:
• the orally disintegrating tablet composition comprises;
• formulations of this example are manufactured according to the process described above in the description.
• Orally disintegrating tablets of the Ex.1 are also tested according to their "Carr compressibility" and "angle of response” as they are also shown in Table 1.
• Common indices of flowability are the Carr index and the angle of repose.
• the increase in bulk density of a powder is related to the cohesiveness of a powder. So measurement of the bulk density of a powder is essential to define the flow characteristics.
• the Carr index gives us the guidance for powder flowability. A lower Carr index of excipients is more desirable for acceptable powder flow.
• Carr Index Classification and Powder Flowability is shown below; Carr Index (compressibility) (%) Flow 5 - 12 Free flowing 12 - 16 Good 18 - 21 Fair 23 - 35 Poor 33 - 38 Very poor > 40 Extremely poor
• Angle of response is a common method used to measure powder flow with small sample quantity. The angles less than 30° are usually indicative of good flow, while powders with angles greater than 40° are likely to be problematic.
• the ultimate goal of flow analysis is to identify the powder or powder blend that provides the least weight variation in the finished tablet. The more fluid the powder is, the more efficiently and reproducibly it should fill the die cavities of a tablet press. This more efficient and reproducible die fill should be reflected in increased tablet weights and reduced intertablet weight variation.
• Table 1 Example 1 Test Results Harndness (Newton) 20-50 Friability (%) ⁇ 0,45 Disintegration time (sec) 20 Carr Compressibilty (%) 5-12 Angle of response ⁇ 30 °

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• 2010
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